Assistant Document Control - 2nd Shift

Role: Document Control Specialist supporting documentation compliance in a pharmaceutical manufacturing setting. Responsibilities: manage electronic and paper document control systems, distribute and track approved documentation, maintain databases, prepare and distribute controlled documents, ensure documentation accuracy and compliance, and assist with audits and regulatory documentation. Requirements: High School diploma or GED; less than one year manufacturing experience; proficiency in cGMP principles and MS Office (Word, Excel, Access). Preferred: Associate degree. High-Value: pharmaceutical manufacturing, cGMP compliance, document management, validation and regulatory support. WorkSetup: 2nd shift, Monday to Friday, 3:00pm–11:30pm.